Anthony R Fehr
Affiliations: | University of Kansas, Lawrence, KS, United States |
Area:
Coronaviruses, ADP-ribosylationGoogle:
"Anthony Fehr"Parents
Sign in to add mentor| James L. Van Etten | research assistant | 2002-2005 | University of Nebraska - Lincoln (Chemistry Tree) | |
| (Undergraduate Research Assistant) | ||||
| Dong Yu | grad student | 2005-2011 | Washington University | |
| (The role of viral protein pUL21a in human cytomegalovirus infection.) | ||||
| Stanley Perlman | post-doc | 2012-2018 | University of Iowa Carver College of Medicine | |
Children
Sign in to add trainee| Catherine Kerr | grad student | 2019- | University of Kansas |
| Joseph O'Connor | grad student | 2020- | University of Kansas |
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Publications
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| Otter CJ, Bracci N, Parenti NA, et al. (2024) SARS-CoV-2 nsp15 endoribonuclease antagonizes dsRNA-induced antiviral signaling. Proceedings of the National Academy of Sciences of the United States of America. 121: e2320194121 |
| Kerr CM, Pfannenstiel JJ, Alhammad YM, et al. (2024) Mutation of highly conserved residues in loop 2 of the coronavirus macrodomain demonstrates that enhanced ADP-ribose binding is detrimental to infection. Biorxiv : the Preprint Server For Biology |
| Wazir S, Parviainen TAO, Pfannenstiel JJ, et al. (2023) Discovery of 2-amide-3-methylester thiophenes that target SARS-CoV-2 Mac1 and repress coronavirus replication, validating Mac1 as an anti-viral target. Biorxiv : the Preprint Server For Biology |
| Otter CJ, Bracci N, Parenti NA, et al. (2023) SARS-CoV-2 nsp15 endoribonuclease antagonizes dsRNA-induced antiviral signaling. Biorxiv : the Preprint Server For Biology |
| O'Connor JJ, Ferraris D, Fehr AR. (2023) An Update on the Current State of SARS-CoV-2 Mac1 Inhibitors. Pathogens (Basel, Switzerland). 12 |
| O'Connor JJ, Voth L, Athmer J, et al. (2023) Two Commercially Available Blood-Stabilization Reagents Serve as Potent Inactivators of Coronaviruses. Pathogens (Basel, Switzerland). 12 |
| Kerr CM, Parthasarathy S, Schwarting N, et al. (2023) PARP12 is required to repress the replication of a Mac1 mutant coronavirus in a cell- and tissue-specific manner. Journal of Virology. 97: e0088523 |
| Alhammad YM, Parthasarathy S, Ghimire R, et al. (2023) SARS-CoV-2 Mac1 is required for IFN antagonism and efficient virus replication in cell culture and in mice. Proceedings of the National Academy of Sciences of the United States of America. 120: e2302083120 |
| Kerr CM, Parthasarathy S, Schwarting N, et al. (2023) PARP12 is required to repress the replication of a Mac1 mutant coronavirus in a cell and tissue specific manner. Biorxiv : the Preprint Server For Biology |
| Alhammad YM, Parthasarathy S, Ghimire R, et al. (2023) SARS-CoV-2 Mac1 is required for IFN antagonism and efficient virus replication in mice. Biorxiv : the Preprint Server For Biology |